Department of Orthopaedics & Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Guangdong Provincial Key Laboratory of Bone and Cartilage Regenerative Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Biomed Res Int. 2019 Mar 4;2019:7483537. doi: 10.1155/2019/7483537. eCollection 2019.
Previous studies had indicated that interleukin-1 beta (IL-1) gene single nucleotide polymorphisms (SNPs) associate with different inflammatory diseases. However, potential links between these polymorphisms and susceptibility to extremity chronic osteomyelitis (COM) remain unclear. This study aimed to investigate relationships between IL-1 gene polymorphisms (rs16944, rs1143627, rs1143634, and rs2853550) and risks of developing extremity COM in Chinese Han population.
Altogether 233 extremity COM patients and 200 healthy controls were genotyped for the four tag SNPs of the IL-1 gene using the SNapShot genotyping method. Comparisons were performed regarding genotype distribution, mutant allele frequency, and four genetic models (dominant, recessive, homozygous, and heterozygous models) of the four SNPs between the two groups.
Significant associations were identified between rs16944 polymorphism and the risk of developing COM by dominant model ( = 0.026, OR = 1.698, 95% CI 1.065-2.707) and heterozygous model ( = 0.030, OR = 1.733, 95% CI 1.055-2.847). Although no statistical differences were found of rs1143627 polymorphism between the two groups, there existed a trend that rs1143627 may be linked to an elevated risk of developing COM by outcomes of dominant ( = 0.061), homozygous ( = 0.080) and heterozygous ( = 0.095) models. However, no statistical correlations were found between rs1143634 and rs2853550 polymorphisms and susceptibility to COM in Chinese Han population.
To our knowledge, we reported for the first time that IL-1 gene rs16944 polymorphism may contribute to the increased susceptibility to extremity COM in Chinese Han population, with genotype of AG as a risk factor.
先前的研究表明,白细胞介素-1β(IL-1)基因单核苷酸多态性(SNP)与不同的炎症性疾病有关。然而,这些多态性与四肢慢性骨髓炎(COM)易感性之间的潜在联系尚不清楚。本研究旨在探讨白细胞介素-1基因多态性(rs16944、rs1143627、rs1143634 和 rs2853550)与汉族人群四肢 COM 发病风险的关系。
采用 SNapShot 基因分型方法,对 233 例四肢 COM 患者和 200 例健康对照者的 IL-1 基因四个标签 SNP 进行基因分型。比较两组间基因型分布、突变等位基因频率以及四个 SNP 的四种遗传模型(显性、隐性、纯合和杂合模型)。
rs16944 多态性与 COM 发病风险的显性模型( = 0.026,OR = 1.698,95%CI 1.065-2.707)和杂合模型( = 0.030,OR = 1.733,95%CI 1.055-2.847)存在显著关联。虽然 rs1143627 多态性在两组间无统计学差异,但存在趋势表明 rs1143627 可能通过显性( = 0.061)、纯合( = 0.080)和杂合( = 0.095)模型增加 COM 的发病风险。然而,rs1143634 和 rs2853550 多态性与汉族人群 COM 易感性之间无统计学相关性。
据我们所知,我们首次报道白细胞介素-1 基因 rs16944 多态性可能与汉族人群四肢 COM 的易感性增加有关,AG 基因型为危险因素。